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DateTitle 
04/14/18Alnylam Presents New Positive Clinical Results for Givosiran, an Investigational RNAi Therapeutic for the Treatment of Acute Hepatic Porphyrias
− In Randomized, Double-Blind, Placebo-Controlled Phase 1 Study, Monthly Givosiran Demonstrated an Over 80 Percent Lowering of Urinary Aminolevulinic Acid (ALA), a Disease Biomarker, and an Over 75 Percent Decrease in Mean Annualized Porphyria Attack Rate, Relative to Placebo − − Evidence of Enhanced Clinical Activity with Long-Term Treatment of up to 22 Months in Ongoing Phase 1/2 Open-Label Extension (OLE) Study, with an Over 90 Percent Decreas... 
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03/28/18Alnylam Presents New Clinical Results from the APOLLO Phase 3 Study of Patisiran at the 16th International Symposium on Amyloidosis
− Patisiran Demonstrated Improvement of Cardiomyopathy in Prospectively Defined Subgroup of Patients with Cardiac Amyloid Involvement, Relative to Placebo − − Long-term Treatment with Patisiran in Global Open-Label Extension (OLE) Study Demonstrates Maintenance of Efficacy and Consistent Safety − − Degree of Patisiran-Mediated TTR Knockdown Found to Correlate with Neurologic Improvement – − New Phase 1 Data on ALN-TTRsc02, ... 
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03/28/18Alnylam and Collaborators to Present Clinical Study Results in Acute Hepatic Porphyrias (AHPs) at The 53rd International Liver Congress™ of the European Association for the Study of the Liver (EASL)
− Updated Results to be Presented from Clinical Studies of Givosiran, an Investigational RNAi Therapeutic for the Treatment of AHPs − − In Addition, Data to be Presented from EXPLORE Natural History Study Characterizing the Burden of Disease in AHPs − CAMBRIDGE, Mass.--(BUSINESS WIRE)--Mar. 28, 2018-- Alnylam Pharmaceuticals, Inc. (Nasdaq: ALNY), the leading RNAi therapeutics company, announced today that Alnylam scientists and... 
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03/26/18Alnylam Receives European Medicines Agency PRIME Designation for Accelerated Assessment of Lumasiran, an Investigational RNAi Therapeutic for the Treatment of Primary Hyperoxaluria Type 1 (PH1)
− Company Intends to Advance Lumasiran to a Phase 3 Study in Late 2018 − CAMBRIDGE, Mass.--(BUSINESS WIRE)--Mar. 26, 2018-- Alnylam Pharmaceuticals, Inc. (Nasdaq: ALNY), the leading RNAi therapeutics company, announced today that the European Medicines Agency (EMA) has granted access to its Priority Medicines (PRIME) scheme for lumasiran (ALN-GO1), an investigational RNAi therapeutic targeting glycolate oxidase for the treatment of Prim... 
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03/21/18Alnylam to Webcast Presentation at 17th Annual Needham Healthcare Conference
CAMBRIDGE, Mass.--(BUSINESS WIRE)--Mar. 21, 2018-- Alnylam Pharmaceuticals, Inc. (Nasdaq: ALNY), the leading RNAi therapeutics company, announced today that management will present a company overview at the 17th Annual Needham Healthcare Conference on Wednesday, March 28, 2018 at 10:00 am ET at the Westin Grand Central Hotel in New York City. A live audio webcast of the presentation will be available on the Investors section of the ... 
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03/21/18Regeneron and Alnylam Pharmaceuticals Announce Collaboration to Discover New Treatments for Nonalcoholic Steatohepatitis (NASH)
Collaboration based on new findings from the Regeneron Genetics Center® showing variant in HSD17B13 gene is associated with reduced risk of chronic liver diseases TARRYTOWN, N.Y. and CAMBRIDGE, Mass., March 21, 2018 /PRNewswire/ -- Regeneron Pharmaceuticals, Inc. (NASDAQ: REGN) and Alnylam Pharmaceuticals, Inc. (NASDAQ: ALNY) today announced a collaboration to identify RNAi therapeutics for the chronic liver disease nonalcoholic steatohepatitis (NASH) and potentially other related diseases.... 
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03/14/18Alnylam to Report New Clinical Results from the APOLLO Phase 3 Study of Patisiran at the 16th International Symposium on Amyloidosis
CAMBRIDGE, Mass.--(BUSINESS WIRE)--Mar. 14, 2018-- Alnylam Pharmaceuticals, Inc. (Nasdaq:ALNY), the leading RNAi therapeutics company, today announced that additional results from the APOLLO Phase 3 study of patisiran, an investigational therapeutic for the treatment of hereditary ATTR (hATTR) amyloidosis, will be presented at the 16th International Symposium on Amyloidosis (ISA), being held March 26-29, 2018 in Kumamoto, Japan. In addition, new d... 
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03/13/18Alnylam Unveils Resources to ‘Bridge the Gap’ in Knowledge of Hereditary ATTR (hATTR) Amyloidosis Among Families at Risk
— hATTRBridge.com features “Living a Rare Life” — one family’s story of living with this rare, genetic condition and the power of discussing family health history — CAMBRIDGE, Mass.--(BUSINESS WIRE)--Mar. 13, 2018-- For many people living with a rare disease, such as hereditary ATTR (hATTR) amyloidosis, it can take years to be accurately diagnosed. Moreover, many may not realize that the symptoms they are experiencing can be tied to their fami... 
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03/12/18Alnylam Retains Global Rights to Lumasiran, an Investigational RNAi Therapeutic for the Treatment of Primary Hyperoxaluria Type 1 (PH1)
− Company Plans to Accelerate Development with Phase 3 Start in Late 2018 − − Lumasiran Granted Breakthrough Therapy Designation by the United States Food and Drug Administration − CAMBRIDGE, Mass.--(BUSINESS WIRE)--Mar. 12, 2018-- Alnylam Pharmaceuticals, Inc. (Nasdaq: ALNY), the leading RNAi therapeutics company, announced today that Sanofi Genzyme has declined its opt-in for the development and commercialization of lumasiran ... 
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03/06/18Alnylam to Webcast Presentations at Upcoming March Investor Conferences
CAMBRIDGE, Mass.--(BUSINESS WIRE)--Mar. 6, 2018-- Alnylam Pharmaceuticals, Inc. (Nasdaq: ALNY), the leading RNAi therapeutics company, announced today that management will present company overviews at the following conferences: Cowen and Company 38th Annual Healthcare Conference on Tuesday, March 13, 2018 at 12:00 pm ET at the Boston Marriott Copley Place in Boston Barclays Global Healthcare Conferenc... 
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02/08/18Alnylam Pharmaceuticals Reports Fourth Quarter and Full Year 2017 Financial Results and Highlights Recent Period Activity
– Reported Final Results from APOLLO Phase 3 Study and Completed Filings of New Drug Application (NDA) and Marketing Authorisation Application (MAA) for Patisiran, with an Expected Commercial Launch in U.S. and Europe in Mid- and Late 2018, Respectively – – Advanced Three Additional RNAi Therapeutics in Phase 3 Development, Including Givosiran in ENVISION, Inclisiran in ORION-9, -10, and -11, and Restart of Fitusiran in ATLAS – – S... 
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02/05/18Alnylam to Webcast Presentations at Upcoming February Investor Conferences
CAMBRIDGE, Mass.--(BUSINESS WIRE)--Feb. 5, 2018-- Alnylam Pharmaceuticals, Inc. (Nasdaq: ALNY), the leading RNAi therapeutics company, announced today that management will present company overviews at the following conferences: 20th Annual BIO CEO & Investor Conference on Monday, February 12, 2018 at 10:45 am ET at the Marriott Marquis in New York City Leerink Partners 7th Annual Global Healthcare... 
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02/01/18Alnylam to Webcast Conference Call Discussing Fourth Quarter and Full Year 2017 Financial Results
CAMBRIDGE, Mass.--(BUSINESS WIRE)--Feb. 1, 2018-- Alnylam Pharmaceuticals, Inc. (Nasdaq: ALNY), the leading RNAi therapeutics company, announced today that it will report financial results for the fourth quarter and year ending December 31, 2017 on Thursday, February 8, 2018, before the U.S. financial markets open. Management will provide an update on the Company and discuss fourth quarter and year-end 2017 results as well as expectations ... 
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02/01/18Alnylam Announces FDA Acceptance of New Drug Application (NDA) and Priority Review Status for Patisiran, an Investigational RNAi Therapeutic for the Treatment of Hereditary ATTR (hATTR) Amyloidosis
– PDUFA date set for August 11, 2018 – CAMBRIDGE, Mass.--(BUSINESS WIRE)--Feb. 1, 2018-- Alnylam Pharmaceuticals, Inc. (Nasdaq: ALNY), the leading RNAi therapeutics company, announced today that the U.S. Food and Drug Administration (FDA) has accepted for filing its New Drug Application (NDA) for patisiran, an investigational RNAi therapeutic targeting transthyretin (TTR) for the treatment of hereditary ATTR (hATTR) amyloidosis. The FD... 
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01/25/18Alnylam Announces EMA Acceptance of Marketing Authorisation Application (MAA) for Patisiran for the Treatment of Hereditary ATTR (hATTR) Amyloidosis
– EMA Will Evaluate MAA Under Accelerated Assessment – CAMBRIDGE, Mass.--(BUSINESS WIRE)--Jan. 25, 2018-- Alnylam Pharmaceuticals, Inc. (Nasdaq: ALNY), the leading RNAi therapeutics company, announced today that the European Medicines Agency (EMA) has accepted the Marketing Authorisation Application (MAA) and initiated its review for patisiran, an investigational RNAi therapeutic targeting transthyretin (TTR) for the treatment of hereditary AT... 
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01/07/18Alnylam Announces 2018 Corporate Goals
Patisiran Expected to be First Commercially Available RNAi Therapeutic in Mid-2018 Restructured Sanofi Alliance Provides Alnylam with Global Commercial Footprint for ATTR Amyloidosis Givosiran Interim Phase 3 Data Expected in Mid-2018 and U.S. New Drug Application Filing Anticipated in Late 2018 Company Plans to Advance Three Additional Phase 3 Programs: Fitusiran, Inclisiran, and ALN-TTRsc02 Company Updates ... 
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01/07/18Alnylam and Sanofi Enter into Strategic Restructuring of RNAi Therapeutics Rare Disease Alliance
– Restructuring Enables Streamlined Development and Optimization of Commercial Opportunities for ATTR Amyloidosis and Hemophilia Programs – – Alnylam Obtains Global Rights for Investigational ATTR Amyloidosis Programs: Patisiran and ALN-TTRsc02 – – Sanofi Obtains Global Rights for Investigational Therapeutic Fitusiran in Hemophilia and Other Rare Bleeding Disorders – – Alnylam to Host Conference Call Today, Sunday, January 7 at 4:... 
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01/04/18Alnylam Expands Alnylam Act™ Program to Include No-Charge Third-Party Genetic Testing and Counseling for People at Risk for Acute Hepatic Porphyrias
– Individuals with Acute Hepatic Porphyrias (AHPs), a Family of Ultra-Rare Genetic Diseases, are Often Misdiagnosed and May Experience an Average Delay in Diagnosis of 15 Years – CAMBRIDGE, Mass.--(BUSINESS WIRE)--Jan. 4, 2018-- Alnylam Pharmaceuticals, Inc. (Nasdaq: ALNY), the leading RNAi therapeutics company, today announced it has expanded the Alnylam Act™ program to include no-charge, third-party genetic testing and counseling for... 
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01/02/18Alnylam to Webcast Presentation at 36th Annual J.P. Morgan Healthcare Conference
CAMBRIDGE, Mass.--(BUSINESS WIRE)--Jan. 2, 2018-- Alnylam Pharmaceuticals, Inc. (Nasdaq: ALNY), the leading RNAi therapeutics company, today announced that management will present a company overview at the 36th Annual J.P. Morgan Healthcare Conference on Monday, January 8, 2018 at 8:00 am PT (11:00 am ET) at The Westin St. Francis in San Francisco. In addition, the company will webcast the Q&A breakout session immediately following its present... 
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